richard sinke
richard sinke
Professor of Genome Analysis, dept. Genetics (MGE), University Medical Center Groningen
Verified email at - Homepage
Cited by
Cited by
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q
SC Bakker, EM Van der Meulen, JK Buitelaar, LA Sandkuijl, DL Pauls, ...
The American Journal of Human Genetics 72 (5), 1251-1260, 2003
Targeted next‐generation sequencing can replace Sanger sequencing in clinical diagnostics
B Sikkema‐Raddatz, LF Johansson, EN de Boer, R Almomani, LG Boven, ...
Human mutation 34 (7), 1035-1042, 2013
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis
BPC Van de Warrenburg, RJ Sinke, CC Verschuuren–Bemelmans, ...
Neurology 58 (5), 702-708, 2002
Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder
K Zhou, A Dempfle, M Arcos‐Burgos, SC Bakker, T Banaschewski, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008
Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes
N Lowe, A Kirley, Z Hawi, P Sham, H Wickham, CJ Kratochvil, SD Smith, ...
The American Journal of Human Genetics 74 (2), 348-356, 2004
Association between an agouti-related protein gene polymorphism and anorexia nervosa
T Vink, A Hinney, AA Van Elburg, SHM Van Goozen, LA Sandkuijl, ...
Molecular psychiatry 6 (3), 325-328, 2001
The human E48 antigen, highly homologous to the murine Ly-6 antigen ThB, is a GPI-anchored molecule apparently involved in keratinocyte cell-cell adhesion.
RH Brakenhoff, M Gerretsen, EM Knippels, M Van Dijk, H Van Essen, ...
The Journal of cell biology 129 (6), 1677-1689, 1995
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy
KY van Spaendonck-Zwarts, A Posafalvi, MP van den Berg, ...
European heart journal 35 (32), 2165-2173, 2014
Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart
D Schultz, G Mikala, A Yatani, DB Engle, DE Iles, B Segers, RJ Sinke, ...
Proceedings of the National Academy of Sciences 90 (13), 6228-6232, 1993
Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy
K Neveling, LA Martinez-Carrera, I Hölker, A Heister, A Verrips, ...
The American Journal of Human Genetics 92 (6), 946-954, 2013
Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch–French cohort
BPC van de Warrenburg, H Hendriks, A Dürr, MCA van Zuijlen, ...
Annals of neurology 57 (4), 505-512, 2005
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23
G Bakalkin, H Watanabe, J Jezierska, C Depoorter, ...
The American Journal of Human Genetics 87 (5), 593-603, 2010
Intermediate CAG repeat lengths (53, 54) for MJD/SCA3 are associated with an abnormal phenotype
N Van Alfen, RJ Sinke, MJ Zwarts, A Gabreëls‐Festen, P Praamstra, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19
A Duarri, J Jezierska, M Fokkens, M Meijer, HJ Schelhaas, ...
Annals of neurology 72 (6), 870-880, 2012
An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia
BJ Jungerius, MLC Hoogendoorn, SC Bakker, R Van't Slot, AF Bardoel, ...
Molecular psychiatry 13 (11), 1060-1068, 2008
Overrepresentation of chromosome 12p sequences and karyotypic evolution in i (12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization
RF Suijkerbuijk, RJ Sinke, AM Meloni, JM Parrington, J Van Echten, ...
Cancer genetics and cytogenetics 70 (2), 85-93, 1993
Peripheral nerve involvement in spinocerebellar ataxias
BPC van de Warrenburg, NC Notermans, HJ Schelhaas, N van Alfen, ...
Archives of neurology 61 (2), 257-261, 2004
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family
BPC Van de Warrenburg, DS Verbeek, SJ Piersma, FAM Hennekam, ...
Neurology 61 (12), 1760-1765, 2003
Neuregulin 1: genetic support for schizophrenia subtypes
SC Bakker, MLC Hoogendoorn, JP Selten, W Verduijn, PL Pearson, ...
Molecular psychiatry 9 (12), 1061-1063, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3
DS Verbeek, BP Van De Warrenburg, P Wesseling, PL Pearson, ...
Brain 127 (11), 2551-2557, 2004
The system can't perform the operation now. Try again later.
Articles 1–20